Arlotta Paola, Molyneaux Bradley J, Chen Jinhui, Inoue Jun, Kominami Ryo, Macklis Jeffrey D
MGH-HMS Center for Nervous System Repair, Departments of Neurosurgery and Neurology, Program in Neuroscience and Harvard Stem Cell Institute, Harvard Medical School, Massachusetts General Hospital, Boston, MA 02114, USA.
Neuron. 2005 Jan 20;45(2):207-21. doi: 10.1016/j.neuron.2004.12.036.
Within the vertebrate nervous system, the presence of many different lineages of neurons and glia complicates the molecular characterization of single neuronal populations. In order to elucidate molecular mechanisms underlying the specification and development of corticospinal motor neurons (CSMN), we purified CSMN at distinct stages of development in vivo and compared their gene expression to two other pure populations of cortical projection neurons: callosal projection neurons and corticotectal projection neurons. We found genes that are potentially instructive for CSMN development, as well as genes that are excluded from CSMN and are restricted to other populations of neurons, even within the same cortical layer. Loss-of-function experiments in null mutant mice for Ctip2 (also known as Bcl11b), one of the newly characterized genes, demonstrate that it plays a critical role in the development of CSMN axonal projections to the spinal cord in vivo, confirming that we identified central genetic determinants of the CSMN population.
在脊椎动物的神经系统中,存在许多不同谱系的神经元和神经胶质细胞,这使得单个神经元群体的分子特征变得复杂。为了阐明皮质脊髓运动神经元(CSMN)特化和发育的分子机制,我们在体内发育的不同阶段纯化了CSMN,并将它们的基因表达与另外两种纯皮质投射神经元群体进行比较:胼胝体投射神经元和皮质顶盖投射神经元。我们发现了对CSMN发育可能具有指导作用的基因,以及被CSMN排除且仅限于其他神经元群体的基因,即使是在同一皮质层内。对新鉴定的基因之一Ctip2(也称为Bcl11b)的无效突变小鼠进行的功能丧失实验表明,它在体内CSMN轴突向脊髓的投射发育中起关键作用,证实我们鉴定出了CSMN群体的核心遗传决定因素。